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Volume 54, Issue 2, Pages 307-317 (August 2009)


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Oral Nicorandil to Reduce Cardiac Death After Coronary Revascularization in Hemodialysis Patients: A Randomized Trial

Masato Nishimura, MD, PhD1Corresponding Author Informationemail address, Toshiko Tokoro, MD, PhD2, Masasya Nishida, MD3, Tetsuya Hashimoto, MD3, Hiroyuki Kobayashi, MD3, Ryo Imai, MD, PhD4, Satoru Yamazaki, MD5, Koji Okino, MD, PhD6, Noriyuki Iwamoto, MD3, Hakuo Takahashi, MD, PhD7, Toshihiko Ono, MD3

Received 24 November 2008; accepted 31 March 2009. published online 18 June 2009.

Background

Survival after invasive coronary revascularization is worse in patients with chronic kidney disease than in patients without chronic kidney disease. We examined whether oral administration of nicorandil, a hybrid nitrate and adenosine triphosphate–sensitive potassium channel opener, could improve outcome after coronary revascularization in hemodialysis patients.

Study Design

Open-labeled prospective randomized trial.

Setting & Participants

Maintenance hemodialysis patients who underwent percutaneous coronary artery intervention and had complete coronary revascularization (absence of both restenosis and de novo coronary lesion) at coronary arteriography 6 months later. Enrollment occurred between January 1, 2002, and December 31, 2004.

Interventions

Treatment with or without oral administration of nicorandil, 15 mg/d.

Outcomes & Measurements

The primary end point was cardiac death (sudden cardiac death or death from acute myocardial infarction or congestive heart failure). The secondary end point was all-cause death. End-point adjudication was performed masked to the intervention.

Results

129 patients (91 men, 38 women) with a mean age of 66 ± 9 (SD) years. During a 2.7 ± 1.5-year follow-up, 26 died of cardiac events (acute myocardial infarction, 6; congestive heart failure, 5; sudden cardiac death, 15), and 12 died of noncardiac causes. Cardiac death–free survival rates were greater in the nicorandil group than in the control group (P = 0.009; at 3 years, 86.6% in the nicorandil group and 70.7% in the control group). All-cause death–free survival rates were also greater in the nicorandil group than in the control group (P = 0.01; at 3 years, 79.2% in the nicorandil group versus 60.5% in the control group). Additional percutaneous coronary artery intervention was performed in 6 participants in the nicorandil group and 2 participants in the control group. No serious side effects of nicorandil were reported during the course of the study.

Limitations

Small sample size and open-label design.

Conclusions

Oral administration of nicorandil may reduce cardiac death and improve the survival of hemodialysis patients after coronary revascularization.

1 Cardiovascular Division, Toujinkai Hospital, Kyoto, Japan

2 Division of Nephrology, Toujinkai Hospital, Kyoto, Japan

3 Division of Urology, Toujinkai Hospital, Kyoto, Japan

4 Division of Orthopedics, Toujinkai Hospital, Kyoto, Japan

5 Toujinkai Clinic, Kyoto, Japan

6 Toujinkai Satellite Clinic, Kyoto, Japan

7 Department of Clinical Sciences and Laboratory Medicine, Kansai Medical University, Osaka, Japan

Corresponding Author InformationAddress correspondence to Masato Nishimura, MD, PhD, Cardiovascular Division, Toujinkai Hospital, 83-1, Iga, Momoyama-cho, Fushimi-ku, Kyoto 612-8026, Japan

 Originally published online as doi: 10.1053/j.ajkd.2009.03.025 on June 18, 2009.

 Trial registration: www.ClinicalTrials.gov; study number: NCT00848562.

PII: S0272-6386(09)00723-9

doi:10.1053/j.ajkd.2009.03.025


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